Clinical trials

60

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Metacognitive Strategy Training Intervention for Transition-Age Youth With Cerebral Palsy

This exploratory randomized controlled trial will examine the feasibility and preliminary effects of a remote PREP intervention compared to an attention control for transition-age youth with cerebral palsy and their caregivers. Youth-caregiver dyads will complete remote baseline assessments and be randomized to a 12-week intervention or attention control, with weekly virtual sessions. Feasibility outcomes will be primary, with secondary outcomes exploring preliminary efficacy. Post-intervention assessments and optional interviews will be conducted remotely to capture outcomes and participant experiences.

Participants needed: 24
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Aug 19, 2026Locations: 1
Eligibility criteria

Youth aged 13 -17 with CP and one primary parent, guardian, or caregiver aged 18... [+4]

Youth with profound intellectual disability [+2]

Status: Recruiting

Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure

The study is to prospectively compare absorbable sutures with non-absorbable sutures used for capsular repair during hip arthroscopic procedures. Major outcomes will be measured using three questionnaires ((1) International Hip Outcome Tool-12 (iHOT-12), (2) modified Harris hip score, (3) hip outcome score) in addition to the standard of care set of 9 questionnaires. The other major outcome will be any radiographic heterotrophic ossification at the 6-month follow-up time point.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Aug 10, 2026Locations: 1
Eligibility criteria

Subjects 18 years of age and older. [+1]

Subjects less than 18 years of age. [+2]

Status: Not yet recruiting

Growth Hormone Resistance of Beta-cells

The purpose of the research study is to better understand how beta-cells (cells in the pancreas that make insulin and help regulate blood sugar) respond to growth hormone in people with impaired fasting glucose or impaired glucose tolerance at the University of Missouri. The aim of the study is to advance understanding of how growth hormone affects beta-cells and risk factors for developing type 2 diabetes.

Participants needed: 10
Trial details
Age: 18-59Biological sex: AllType: ObservationalSponsor: University of Missouri-ColumbiaUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

body mass index >18.5kg/m2 and <45.9kg/m2 [+1]

pregnant, planning to become pregnant during the study, or breastfeeding [+11]

Status: Recruiting

Effects of Grape Consumption on the Immune-Gut Axis in Obesity

This study is investigating the benefits of whole freeze-dried grape powder consumption on the immune-gut axis in adults with obesity.

Participants needed: 50
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 31, 2026Locations: 1
Eligibility criteria

Age: 18-60 years [+6]

Study food allergies [+12]

Status: Not yet recruiting

Effects of Sirolimus on Asymptomatic ApoE4 Carriers

Alzheimer's disease is a devastating neurodegenerative disease characterized by accumulation of clumps (also called plaques) and bundles of fibers (also called tangles) in the brain, for which there is currently no cure. Sirolimus (Rapamycin) is an FDA-approved medication which may improve the blood flow to the brain. The purpose of the clinical trial is to find out whether sirolimus can help improve blood flow and energy use in the brain in women ages 45 to 65 who have the ApoE4 gene, a gene which increases the risk of developing Alzheimer's disease later in life. There will be two arms in this trail, a sirolimus arm and a placebo arm. A placebo is a pill that looks like the study drug, but it does not have any real medicine in it. Participants will be randomized to one arm or the other, but not to both arms. Three study visits over a 12-week period are required. Participants will: (i) Complete some questionnaires about how well you think; (ii) Complete genetic testing for the ApoE4 gene; (iii) Have blood work, blood pressure and height and weight collected; (iv) Take either Sirolimus or a placebo daily, by mouth, for approximately 4 weeks; (v) Keep a diary of when the sirolimus or placebo is taken; (vi) Complete 2 Magnetic Resonance Imaging (MRI) exams

Participants needed: 225
Trial details
Phase: Phase 1Age: 45-65Biological sex: FemaleType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 30, 2026Locations: 1
Eligibility criteria

Willing and able to provide informed consent [+9]

Diagnosis of mild cognitive impairment (MCI), dementia, or Alzheimer's disease [+25]

Status: Recruiting

Talar Osteochondral Lesions With Pilon Fractures

Patients with pilon fractures have a high incidence of talar osteochondral lesions. In this study, patients will undergo ankle arthroscopy at the time of external fixation. The objective is to help determine the incidence of these lesions with pilon fractures and to see if these nano-arthroscopy results change the plan for definitive treatment.

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 30, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years (skeletally mature) Tibial plafond fractures with impaction of th...

Prior ankle surgery [+6]

Status: Not yet recruiting

Impact of Biphasic Cuirass Ventilation Compared to Non Invasive Ventilation in High Risk Extubations

subjects on mechanical ventilator who are about to be extubated to Non invasive ventilation because the physician thinks they are high risk for failure will be approached and consented for our study. Once randomized they will either be on the standard of care Non invasive arm or the intervention arm which would mean they are placed on the Biphasic cuirass ventilation.

Participants needed: 50
Trial details
Age: 19-80Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 28, 2026
Eligibility criteria

High risk extubation patients in the Medical Intensive care units who are being...

Age <18 or >80 [+7]

Status: Not yet recruiting

Beta3-adrenergic Receptors and Cardiovascular Function in Aging Women

To determine if vascular beta3 adrenergic receptors are present and functional in aging women and can be targeted to attenuate sympathetic vasoconstriction and enhance vascular function in aging women.

Participants needed: 60
Trial details
Phase: Early Phase 1Age: 18-70Biological sex: FemaleType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

Healthy women, [+3]

Assigned male at birth, [+12]

Status: Not yet recruiting

Interplay of Central and Peripheral Vascular Effects of Insulin in Obesity

Determine the impact of obesity with insulin resistance on the neurovascular response to brain insulin stimulation.

Participants needed: 64
Trial details
Phase: Early Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

18 to 65 years of age [+6]

Pregnancy, breastfeeding [+13]

Status: Recruiting

Impact of Sleep Restriction on Blood Pressure Reactivity

The purpose of the research study is to examine the effects of shortened sleep on blood pressure.

Participants needed: 45
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

Healthy adult men and women [+5]

No acute or chronic conditions [+3]

Status: Recruiting

Sex Disparities in Hypoxic Vasodilation and Impact of Obesity

The purpose of this project is to examine key mechanisms contributing to sex-differences in hypoxic vasodilation and the impact of obesity, with particular emphasis on the sympathetic nervous system.

Participants needed: 72
Trial details
Phase: Early Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

BMI >18 kg/m2

Pregnancy, breastfeeding [+9]

Status: Recruiting

Pars Healing on MRI

The goal of this clinical trial is to learn more about the natural healing process of pars stress injuries in adolescents and young adults by documenting bony bridging across stress fractures using Magnetic Resonance Imaging (MRI). It is hypothesized that many of these injuries can and will heal with appropriate rest and rehabilitation. Long-term, it is hoped that follow-up MRI exams can help guide clinical management by visualizing the healing and allowing individuals to return to play after bony bridging has occurred. Participants will be asked to undergo serial MRI scans over the course of a 12-month period and answer a brief questionnaire at each visit.

Participants needed: 40
Trial details
Age: 12-30Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 22, 2026Locations: 1
Eligibility criteria

12-30 years old [+2]

Prior lumbar surgery [+4]

Status: Recruiting

Propranolol in Primary Progressive Aphasia

The purpose of this study is to find out how the language of people with Primary Progressive Aphasia is affected by Propranolol. Propranolol is not FDA approved for the treatment of Primary Progressive Aphasia. Propranolol is FDA approved for the treatment of heart conditions such as blood pressure. This research is being done because there are currently no drug treatment options for language impairments and anxiety often experienced by people with Primary Progressive Aphasia.

Participants needed: 30
Trial details
Phase: Early Phase 1Age: 50+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jul 17, 2026Locations: 1
Eligibility criteria

1. Age: 50 and older [+2]

1. Unable to provide consent [+13]

Status: Recruiting

Baker Gordon Syndrome Natural History Study

The goal of this study is to conduct a prospective, longitudinal assessment of the natural clinical progression of children and adults with Synaptotagmin1-Associated Neurodevelopmental Disorder also known as Baker Gordon Syndrome (BAGOS). This will be performed by acquiring baseline measurements and developing effective outcome measures and diagnostic tools for the disorder, to prepare the healthcare system for future clinical trials.

Participants needed: 50
Trial details
Age: 0-99Biological sex: AllType: ObservationalSponsor: University of Missouri-ColumbiaUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Genetically confirmed diagnosis of Baker Gordon syndrome. [+3]

>18 years. [+4]

Status: Recruiting

Subjective Intraoperative Use of Epidural Steroid Administration Following Discectomy

The purpose of this study is to determine a grading system for inflammation in lumbar disc herniation and which groups, if any, benefit most from the administration of an intra-operative epidural steroid.

Participants needed: 200
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Presenting to the University of Missouri hospital system - including the Univers... [+3]

Concomitant spinal stenosis, segmental instability, or spondylolisthesis [+4]

Status: Recruiting

Growth Hormone Resistance of Beta-cells in People With a Family History of Type 2 Diabetes

The purpose of the research study is to better understand how beta-cells (cells in the pancreas that make insulin and help regulate blood sugar) respond to growth hormone in people with a family history of type 2 diabetes at the University of Missouri. Our aim is to advance understanding of how growth hormone affects beta-cells and risk factors for developing type 2 diabetes.

Participants needed: 30
Trial details
Age: 18-59Biological sex: AllType: ObservationalSponsor: University of Missouri-ColumbiaUpdated: May 11, 2026Locations: 1
Eligibility criteria

18 to 59 years old [+3]

Pregnant, planning to become pregnant during the study, or breastfeeding [+11]

Status: Recruiting

Growth Hormone Resistance of Beta-cells A

The purpose of the research study is to better understand how beta-cells (cells in the pancreas that make insulin and help regulate blood sugar) respond to growth hormone in people with a personal history of gestational diabetes (high blood sugar in pregnancy) at the University of Missouri. The aim of the study is to advance understanding of how growth hormone affects beta-cells and risk factors for developing gestational diabetes.

Participants needed: 30
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: University of Missouri-ColumbiaUpdated: May 11, 2026Locations: 1
Eligibility criteria

Singleton, full term pregnancy within the past 5 years [+3]

Pregnant, planning to become pregnant during the study, or breastfeeding [+11]

Status: Recruiting

High Protein Diet and Atherosclerosis

Atherosclerosis is the underlying cause of the majority of cardiovascular diseases, including myocardial infarction and strokes, and results in tremendous morbidity and mortality. A Western-type diet is a major risk factor for atherosclerosis because of the high saturated fat, cholesterol, and refined carbohydrate contents. Dietary strategies to reduce cardiovascular disease burden therefore focus on restriction of saturated fat, cholesterol, and refined carbohydrates whereas "lean" protein intake is recommended and has become popular. However, results from studies conducted in animal models suggest high dietary protein intake is also atherogenic. The investigators' extensive preliminary data in animal models show that dietary protein increases atherosclerotic plaque formation and size and promotes necrotic core formation, a characteristic of rupture-prone plaques. The goal of the current proposal is to provide deeper insights into the relationship between protein intake and the pathogenesis of atherosclerosis by studying the mechanisms involved in protein-mediated atherogenesis and formation of necrotic plaques. The overarching hypothesis is that high protein intake drives atherosclerosis via leucine-mediated mTORC1 signaling in macrophages, which inhibits macrophage mitophagy and aggrephagy and stimulates macrophage proliferation. Furthermore, the investigators hypothesize that proteins from animal sources are more atherogenic than proteins from plant sources, because animal proteins contain more leucine than plant proteins. The investigators will test these hypotheses by using a sophisticated array of experimental strategies, including assays in primary macrophages and human monocyte-derived macrophages and genetically engineered mouse models. In addition, they will begin to translate the results obtained in vitro and in animals to people, and explore approaches to pharmacologically target the pro-atherogenic pathways as novel cardiovascular therapeutics. This proposal represents a paradigm shift in how a Western-type diet affects vascular health which has important implications since many adults in Western societies consume excess protein and dietary protein is heavily marketed for its presumed beneficial health effects.

Participants needed: 24
Trial details
Age: 45-75Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: May 11, 2026Locations: 1
Eligibility criteria

>=45 and <=75 years of age [+1]

<45 and >75 years of age [+11]

Status: Recruiting

Animal and Plant Proteins and Glucose Metabolism

The goal of this proposal is to determine the effect of a high protein diet in which the increase in protein intake is derived from different sources (animal vs plant and protein-rich whole foods vs protein isolates) on: i) liver and muscle insulin sensitivity; ii) the metabolic response to a meal, and iii) 24-h plasma concentration profiles of glucose, glucoregulatory hormones, and protein-derived metabolites purported to cause metabolic dysfunction.

Participants needed: 100
Trial details
Age: 21-70Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: May 8, 2026Locations: 1
Eligibility criteria

age: ≥21 and ≤70 years; [+3]

prediabetes or type 2 diabetes; [+8]

Status: Recruiting

Effect of Drain Care on Infection Rate and Quality of Life in Implant-Based Breast Reconstruction.

The goal of this clinical trial is to learn whether showering with surgical drain tubes in place after first stage breast reconstruction causes increased risk of infection. The main questions it aims to answer are: * Is there an increased risk of infection/complications with showering 48 hours after drain tubes are in place * Does showering after 48 hours with drain tubes in place affect quality of life.

Participants needed: 100
Trial details
Age: 18-100Biological sex: FemaleType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: May 5, 2026Locations: 1
Eligibility criteria

undergoing breast surgery with placement of tissue expander and drains, acceptan...

no existing wounds, previous infections related to implant device if delayed, re...

Status: Recruiting

Evaluation of Cognitive Behavioral Therapy for Insomnia (CBT-I) in Individuals With Mild Traumatic Brain Injury (mTBI)

This study will employ cognitive behavioral therapy for insomnia (CBT-I) among individuals with mild traumatic brain injury (mTBI) who experience sleep disturbances. The research aims to evaluate the effects of CBT-I on sleep, mTBI symptoms, and, in particular, the ability of individuals with mTBI to engage in their desired daily life activities. The main questions this study aims to answer are: 1. Does CBT-I positively impact symptoms of mTBI? 2. Does CBT-I improve functional performance in individuals with mTBI?

Participants needed: 15
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: May 1, 2026Locations: 1
Eligibility criteria

A history of mTBI documented by a physician and sleep problems for more than 4 w... [+2]

History of other neurological or psychological conditions [+3]

Status: Not yet recruiting

Insomnia and Insulin Resistance

Insomnia symptoms are linked to metabolic syndrome (MetS), which includes abnormal glucose metabolism, insulin resistance (IR), and incidence of diabetes. Chronic sleep deficit is a major predictor of disease and early mortality. Further, insomnia is the most common sleep disorder in the United States. The recommended first line of treatment for insomnia is Cognitive Behavioral Therapy for Insomnia (CBT-I). CBT-I is a multidimensional treatment that targets the thoughts and behaviors that perpetuate insomnia symptoms over time. This study will explore CBT-I effects on MetS outcomes (ie. blood pressure, triglycerides, etc.) and provide preliminary evidence that CBT-I impacts IR and fasting glucose concentrations within this population. 20 subjects with insomnia will be recruited. They will be randomly assigned to either CBT-i or sleep hygiene. The intervention is 5 wks. Pre and post intervention, the investigator will have participants fill out a number of questionnaires, a daily sleep diary, 2 weeks of actigraphy measuring sleep and physical activity and there will be a single blood draw at the beginning and the end of the study.

Participants needed: 20
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Apr 28, 2026
Eligibility criteria

Not listed

Status: Recruiting

The Feasibility of a Remote Problem-Solving Intervention for Autistic Adolescents or Young Adults and a Caregiver

This project seeks to evaluate the feasibility and acceptability of a remote metacognitive strategy training intervention in transition-age autistic adolescents and young adults and a primary caregiver. We will also conduct limited efficacy testing.

Participants needed: 24
Trial details
Age: 13-21Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Autistic adolescents aged 13-21 AND one primary parent, guardian, or caregiver a... [+3]

Severe or profound intellectual disability (IQ<35) [+2]

Status: Recruiting

Tumor Cell and DNA Detection in the Blood, Urine and Bone Marrow of Patients With Solid Cancers

Patients with resectable solid primary cancers and even limited number of metastases are potentially curable. However, most patients develop recurrences despite surgery. Circulating and disseminated tumor cell (CTC/DTC) and circulating cell-free (cf) DNA isolation from the blood, urine and bone marrow will increase understanding of cancer spread and advance knowledge to develop individualized therapies.

Participants needed: 620
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of Missouri-ColumbiaUpdated: May 1, 2026Locations: 1
Eligibility criteria

Subjects older than 18 years. [+5]

Pregnant women. [+4]

Status: Recruiting

Skin Preparation for Elective Foot and Ankle Surgery

Surgical site infections (SSIs) make about 31% of all nosocomial infections and they are the most common hospital-acquired infection. For foot and ankle elective interventions, SSI rate is reported between 0.4% and 3.6%. This study will investigate the effectiveness of skin cleaning with isopropyl alcohol and scrubbing with chlorhexidine soap before standard skin preparation in reducing microbial load and surgical site infections for elective foot and ankle surgeries. Current standard of care includes skin preparation with iodine or chlorhexidine solution prior to sterile draping and the start of surgery. Standard of care will be applied to all patients. The use of an additional "pre-scrub" with isopropyl alcohol and scrubbing with chlorhexidine soap will be applied to the experimental group. The control group will receive only the standard of care skin preparation with iodine or chlorhexidine solution prior to draping.

Participants needed: 100
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Apr 27, 2026Locations: 1
Eligibility criteria

patients undergoing elective foot and ankle surgeries [+1]

trauma as the indication for surgery [+5]